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Early detection of cervical cancer using microarray analysis and gene regulatory rules

机译:利用微阵列分析和基因调控规则早期发现宫颈癌

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摘要

The near future in healthcare is the personalized medicine. It is mainly based on the analysis of an individual's genomic biomarkers and their regulation. The origin of many diseases can be revealed by knowing the gene regulation. To achieve this goal analysis of microarray data is essential which helps to collect genomic data and regulation details. This paper advised the analysis of Affymetrix micro array data of cervical cancer that helps in the early detection of cancer. At the end of this analysis phase, differentially expressed genes in cancer samples are identified and perform steps for finding regulation. Through the cellular signaling networks, genes regulate the expression of other genes, which finally results in stable phenotype structures such as tumor or non-tumor cells. Often, tumor and non-tumor cellular network contains some identical cancer-causing genes, but due to the corresponding gene regulatory network (GRN) in tumor networks, they eventually end up in forming the cancerous cells, whereas in non-tumor networks, they do not. The potential for cancer could be detected before it actually happens if we could estimate the basic gene regulatory function rules. This paper applies a mathematical approach to determine such regulatory rules for a set of cells containing cancer causing genes. The approach conferred here is based on the utilization of probabilistic Boolean network model on the selected genes.
机译:在医疗保健领域,不久的将来是个性化药物。它主要基于对个体基因组生物标志物及其调控的分析。通过了解基因调控可以揭示许多疾病的起源。为了实现这一目标,对微阵列数据进行分析至关重要,这有助于收集基因组数据和法规详细信息。本文建议对宫颈癌的Affymetrix微阵列数据进行分析,以帮助早期发现癌症。在此分析阶段的最后,鉴定出癌症样品中差异表达的基因,并执行寻找调控的步骤。通过细胞信号网络,基因调节其他基因的表达,最终产生稳定的表型结构,例如肿瘤或非肿瘤细胞。通常,肿瘤和非肿瘤细胞网络包含一些相同的致癌基因,但是由于肿瘤网络中相应的基因调控网络(GRN),它们最终最终形成癌细胞,而在非肿瘤网络中,它们不要。如果我们可以估计基本的基因调节功能规则,则可以在癌症真正发生之前就发现其潜在可能性。本文采用数学方法来确定一组包含致癌基因的细胞的调控规则。这里提供的方法是基于对所选基因的概率布尔网络模型的利用。

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